Bliss Colao,Annika Liu,Azin Azarfar et al.
Bliss Colao et al.
Sclerosing mediastinitis (SM) is a rare condition characterized by extensive fibrous proliferation within the mediastinum. While some patients remain asymptomatic, others may present with chest pain, dyspnea, hemoptysis, or complications su...
Hip Chondrolysis Due to Enthesitis-Related Juvenile Idiopathic Arthritis Treated Successfully With Adalimumab [0.03%]
阿达木单抗成功治疗的与enthesis炎相关的幼年特发性关节炎导致的髋部软骨溶解
Gosuke Akiyama,Hyonmin Choe,Naomi Kobayashi et al.
Gosuke Akiyama et al.
Coxitis with rapid hip chondrolysis in juvenile patients requires careful diagnosis and treatment. This report describes a case that was initially diagnosed as idiopathic hip chondrolysis (IHC) but finally diagnosed as enthesis-related juve...
Critical Limb Ischaemia in Granulomatosis with Polyangiitis: A Rare but Severe Complication [0.03%]
变应性肉芽肿血管炎的重症并发症——肢体_critical_缺血
Anushka Aggarwal,Rohini Handa,Rakesh Mahajan et al.
Anushka Aggarwal et al.
Granulomatosis with polyangiitis (GPA) is a small-to-medium vessel vasculitis usually presenting with upper airway, pulmonary, and renal involvement. Critical limb ischaemia (CLI) and arterial thrombosis are rare but severe complications of...
Anti-SRP antibody-positive polymyositis complicated by neuromyelitis optica spectrum disorder: A case report and literature review [0.03%]
抗SRP抗体阳性多发性肌炎合并视神经脊髓炎谱系障碍1例及文献复习
Eisuke Tanaka,Mai Kawazoe,Shotaro Masuoka et al.
Eisuke Tanaka et al.
Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune inflammatory demyelinating disease primarily affecting the optic nerves and spinal cord. Polymyositis (PM) is an idiopathic inflammatory myopathy characterized by proximal musc...
Tocilizumab-Induced Bullous Rheumatoid Neutrophilic Dermatitis: A Rare Steroid-Resistant Adverse Effect Managed with Etanercept [0.03%]
托珠单抗引起的类风湿性嗜中性脓疱性皮炎：一种罕见的糖皮质激素抵抗型不良反应，使用英夫利昔治疗有效
Thabuna Sivaprakasam,Molly Lien,Amna Gill et al.
Thabuna Sivaprakasam et al.
Neutrophilic dermatoses (NDs) are a heterogeneous group of inflammatory skin disorders marked by dense, sterile neutrophilic infiltrates. Rheumatoid neutrophilic dermatitis (RND), a rare subtype, is uniquely associated with rheumatoid arthr...
VEXAS syndrome with eosinophilia and pathologically mimicking histiocytosis: A case report [0.03%]
以嗜酸细胞增多为特征并病理上类似组织细胞增生症的VEXAS综合征1例报告
Yasuhisa Murai,Rina Watanabe,Tatsuya Tsurumoto et al.
Yasuhisa Murai et al.
Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic (VEXAS) syndrome is a recently identified autoinflammatory disorder caused by somatic mutations in the UBA1 gene. This report describes the case of a 54-year-old Japanese man with VEX...
Late Diagnosis of Hyperphosphatemic Familial Tumoral Calcinosis in an Adult Male: Lessons from a Misclassified Case [0.03%]
成人男性高磷血症家族性肿瘤钙化病的晚期诊断：一个误分类病例的教训
Ayatallah Abu Jami,Omar Ismail,Fatima Alnaimat
Ayatallah Abu Jami
Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare autosomal recessive disorder caused by multiple genetic mutations, all leading to reduced FGF23 function. It is characterized by hyperphosphatemia, ectopic calcifications, and s...
Successful treatment of pustulotic arthro-osteitis with bimekizumab: A case report [0.03%]
生物克珠单抗治疗疱疹性关节骨炎成功的一例报告
Masahiro Kogami,Rina Takahashi,Ryosuke Shirayanagi et al.
Masahiro Kogami et al.
Pustulotic arthro-osteitis (PAO) is an inflammatory osteoarticular disorder associated with palmoplantar pustulosis (PPP). While anti-TNF-α agents and IL-23 inhibitors have shown efficacy in PAO, the therapeutic potential of bimekizumab (B...
Case Reports: Peficitinib Efficacy in Treating Palmoplantar Pustulosis Induced by Paradoxical Reactions to Golimumab in Two Rheumatoid Arthritis Cases [0.03%]
两例类风湿关节炎患者因戈利木单抗诱发的同形式反应导致掌跖脓疱病的皮科疗效报告：培菲康治疗成功案例
Mari Yamamoto,Waka Yokoyama-Kokuryo,Hiroki Ikai et al.
Mari Yamamoto et al.
A paradoxical reaction refers to a response opposite to the expected effects of drug therapy. Cutaneous paradoxical reactions, which occur with the use of immunosuppressive drugs, are believed to result from treatment-induced cytokine imbal...
Rapidly progressive glucocorticoid-resistant childhood-primary angiitis of the central nervous system positive for HLA-B51 and A26: A case report [0.03%]
抗糖皮质激素的儿童中枢神经系统原发性血管炎伴有HLA-B51和A26阳性迅速进展的一例报告
Yuji Fujita,Kei Ikeda,Sayumi Saida et al.
Yuji Fujita et al.
Primary angiitis of the central nervous system (PACNS) is a rare inflammatory vasculitis localized to the central nervous system. Treatment of severe PACNS often includes glucocorticoids and cyclophosphamide; however, some cases exhibit res...